MedPath

Cabozantinib

Generic Name
Cabozantinib
Brand Names
Cabometyx, Cometriq
Drug Type
Small Molecule
Chemical Formula
C28H24FN3O5
CAS Number
849217-68-1
Unique Ingredient Identifier
1C39JW444G

Overview

Cabozantinib was first approved in 2012 and is a non-specific tyrosine kinase inhibitor. It was initially approved in the US under the brand name Cometriq, which is indicated for the treatment of metastatic medullary thyroid cancer. In 2016, a capsule formulation (Cabometyx) was approved for the treatment of advanced renal cell carcinoma, and this same formulation gained additional approval in both the US and Canada in 2019 for the treatment of hepatocellular carcinoma in previously treated patients.

Background

Cabozantinib was first approved in 2012 and is a non-specific tyrosine kinase inhibitor. It was initially approved in the US under the brand name Cometriq, which is indicated for the treatment of metastatic medullary thyroid cancer. In 2016, a capsule formulation (Cabometyx) was approved for the treatment of advanced renal cell carcinoma, and this same formulation gained additional approval in both the US and Canada in 2019 for the treatment of hepatocellular carcinoma in previously treated patients.

Indication

⑴治疗进展的、不能切除的局部晚期或转移的髓性甲状腺癌。 ⑵用于舒尼替尼(索坦)治疗失败的晚期肾癌。

Associated Conditions

  • Advanced Renal Cell Carcinoma
  • Hepatocellular Carcinoma
  • Metastatic Differentiated Thyroid Cancer
  • Locally advanced Differentiated Thyroid Cancer (DTC)
  • Metastatic Clear Cell Renal Cell Carcinoma (ccRCC)
  • Progressive, metastatic Medullary thyroid cancer

Clinical Trials

View More Clinical Trials

Sign in to access the complete clinical trial database with detailed study information.

Title
Posted
Study ID
Phase
Status
Sponsor
2024/07/01
Phase 2
Recruiting
2024/06/26
Phase 3
Recruiting
ECOG-ACRIN Cancer Research Group
2024/04/22
Phase 2
Terminated
2024/04/15
Phase 3
Recruiting
2024/04/02
Phase 2
Recruiting
2023/12/15
Phase 2
Active, not recruiting
2023/12/05
Phase 1
Recruiting
2023/11/15
Phase 1
Recruiting
2023/09/07
Phase 1
Recruiting
2023/08/23
Phase 2
Active, not recruiting

FDA Drug Approvals

View More FDA Approvals

Sign in to access additional FDA-approved drug information with detailed regulatory data.

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.
Showing 0 of 4 FDA approvals

EMA Drug Approvals

View More EMA Approvals

Sign in to access additional EMA-approved drug information with detailed regulatory data.

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.
Showing 0 of 4 EMA approvals

HSA Drug Approvals

View More HSA Approvals

Sign in to access additional HSA-approved drug information with detailed regulatory data.

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.
Showing 0 of 3 HSA approvals

NMPA Drug Approvals

View More NMPA Approvals

Sign in to access additional NMPA-approved drug information with detailed regulatory data.

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

View More PPB Approvals

Sign in to access additional PPB-approved drug information with detailed regulatory data.

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

View More TGA Approvals

Sign in to access additional TGA-approved drug information with detailed regulatory data.

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.
© Copyright 2025. All Rights Reserved by MedPath